Medline Convenience kits containing recalled Swan-Ganz Catheters OPEN HEART … Recall
Issued July 8, 2026 · Medline Industries, LP
In July 2026, Medline Industries, LP recalled the Medline Convenience kits containing recalled Swan-Ganz Catheters OPEN HEART …, a serious health recall reported by the FDA. Affected owners are eligible for a voluntary. Here is what the hazard is and exactly what to do about it.
Compiled by Dana Whitfield, RecallCheckr
What this means for you
Kits contain Swan-Ganz catheters recalled by Becton Dickinson (BD). BD has received complaints of leaks/breakage involving failures of the (blue) proximal injectate lumen hub on these catheters. This has led to instances of leakage, lumen damage, and breakage, and may lead to infection, medication loss, and/or blood loss.
What you should do
- 1 Stop using Medline Convenience kits containing recalled Swan-Ganz Catheters OPEN HEART … right away.
- 2 Set it aside where it won't be used by mistake.
- 3 Contact Medline Industries, LP to arrange your voluntary. See the official notice below for contact details.
- 4 Keep the product until your remedy is fully processed. You may need it.
Recall details
- Brand
- Medline Industries, LP
- Category
- Health
- Recall date
- July 8, 2026
- Units affected
- Not reported
- Sold at
- US Nationwide distribution in the states of AZ, CA, FL, IL, MO, NJ, OH, OK, TN, TX, WI.
- Recall number
- FDA-Z-2611-2026
- Made in
- United States
- Issuing agency
- FDA
In context
- Medline Industries, LP has 62 recalls in our database, including 8 rated Critical.
- We're tracking 3,673 Health recalls in our database.
- This is the 453rd Health recall we've logged in 2026.